# Alpha Tekniko – FDA Inspection, Dec 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/alpha-tekniko/9577b29b-6da5-424b-85fb-b3ec8210a765
Source feed: FDA_Inspections

> FDA inspection 1034999 of Alpha Tekniko, December 14, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1034999
- Company Name: Alpha Tekniko
- Inspection Date: 2017-12-14
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1310970 - 2026-03-27
- FDA Inspection 1174382 - 2022-06-22

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/nicholas-z-lu/17448aca-e316-424c-b7b2-88c8baffc359)

Company: https://www.keypedia.com/companies/alpha-tekniko/8f9d6c46-17c5-4666-b797-0ebba19eb86b

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7